Lunesta Cost in Idaho 2026: Eszopiclone Prices, Insurance, and Savings

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Lunesta Cost in Idaho 2026: What You Will Actually Pay for Eszopiclone

At a glance

  • Brand list price / ~$140/month (Lunesta, Sunovion)
  • Generic cash price / ~$20/month at Idaho retail pharmacies in 2026
  • Compounded eszopiclone (503A) / $0/month through select telehealth programs
  • Idaho Medicaid coverage / Not covered as of 2025-2026
  • Telehealth prescribing / Legal in Idaho
  • Compounded 503A prescribing / Legal in Idaho via licensed compounding pharmacy
  • Standard dose / 1 mg, 2 mg, or 3 mg oral tablet once at bedtime
  • DEA schedule / Schedule IV controlled substance
  • FDA approval year / 2004 (NDA 021476)
  • Typical trial period shown effective / 6 months (Krystal et al., 2003)

What Does Lunesta Actually Cost in Idaho in 2026?

Brand-name Lunesta's manufacturer list price sits around $140 per month in Idaho, but almost no cash-pay patient pays that figure. Generic eszopiclone, available since 2014, retails for approximately $20 per month at most Idaho pharmacies when a free discount coupon is applied. The spread between list price and actual cash price is one of the largest in the sedative-hypnotic category.

Eszopiclone is the S-enantiomer of zopiclone and received FDA approval in December 2004 under NDA 021476 for the treatment of insomnia characterized by difficulty with sleep onset and sleep maintenance [1]. The drug works on GABA-A receptors similarly to benzodiazepines, though its chemical structure is distinct. Because it is a Schedule IV controlled substance under the Controlled Substances Act, every prescription requires a DEA-registered prescriber, which shapes telehealth access rules in Idaho [2].

Real-world pricing at Idaho pharmacies in early 2026 shows generic eszopiclone at Walgreens, Walmart, and Fred Meyer pharmacies ranging from $18 to $28 for a 30-tablet supply of the 2 mg or 3 mg strength when a GoodRx or RxSaver coupon is presented at the counter. The 1 mg strength, used primarily in older adults or patients with hepatic impairment, may be slightly less. Brand Lunesta is rarely dispensed at this point given near-identical bioequivalence of the generic.

The FDA's bioequivalence standard requires generic manufacturers to demonstrate that their product delivers 80 to 125 percent of the reference drug's area under the concentration-time curve, meaning Idaho patients filling generic eszopiclone receive a therapeutically equivalent product [3].

How Idaho Medicaid Handles Eszopiclone Coverage

Idaho Medicaid does not cover eszopiclone in its preferred drug list as of the 2025-2026 benefit year. This means members enrolled in Idaho Medicaid (administered by the Idaho Department of Health and Welfare) will receive no reimbursement for either brand Lunesta or its generic equivalent without a prior authorization that, in practice, is rarely approved for a Schedule IV hypnotic.

The Idaho Medicaid Preferred Drug List is updated quarterly. Prescribers seeking coverage for a Medicaid member can submit a prior authorization citing clinical necessity, failure of non-pharmacologic interventions such as cognitive behavioral therapy for insomnia (CBT-I), and intolerance or contraindication to covered alternatives [4]. The Centers for Medicare and Medicaid Services notes that states retain flexibility to exclude or restrict Schedule IV sedative-hypnotics from their formularies under the federal Medicaid drug rebate program rules [5].

Patients on Medicare Part D face a similarly fragmented picture. Eszopiclone is excluded from some Part D formularies under the "protected class" exemption gap for sedative-hypnotics. A 2022 CMS analysis found that roughly 40 percent of Part D plans placed non-benzodiazepine hypnotics on Tier 3 or higher, with average copays of $45 to $90 per month after deductible [6]. Idaho Medicare enrollees should check their specific plan's formulary at medicare.gov each October during open enrollment.

The American Academy of Sleep Medicine's 2017 clinical practice guideline on chronic insomnia states: "We suggest that clinicians use eszopiclone as a treatment for sleep onset and sleep maintenance insomnia (versus no treatment) in adults" [7]. That recommendation, however, does not compel state Medicaid programs to cover the drug.

Generic Eszopiclone vs. Brand Lunesta: Is There a Real Difference?

There is no clinically meaningful pharmacokinetic difference between FDA-approved generic eszopiclone and brand Lunesta for most Idaho patients. The key efficacy data behind the brand apply equally to the generic by virtue of the FDA's AB-rated bioequivalence designation [3].

The landmark 6-month trial by Krystal and colleagues (2003, N=788) remains the longest randomized placebo-controlled trial of eszopiclone. Patients randomized to eszopiclone 3 mg nightly showed statistically significant improvements in subjective sleep onset latency (reduction of 12.4 minutes vs. placebo, P<0.001), total sleep time (increase of 46 minutes vs. placebo), and daytime functioning scores over the full 24-week period without evidence of tolerance development [8]. That trial, published in Sleep, was instrumental in FDA approval and continues to anchor prescribing confidence in the drug's long-term safety profile.

A 2007 crossover pharmacokinetic study in Biopharmaceutics and Drug Disposition confirmed that the S-enantiomer is responsible for the drug's hypnotic activity, and that racemic zopiclone's R-enantiomer contributes primarily to side effects including the metallic taste reported by up to 34 percent of users [9]. Patients who tolerate generic eszopiclone well are experiencing the same active compound as brand Lunesta at a fraction of the cost.

Compounded Eszopiclone in Idaho: Legality and Cost

Compounded eszopiclone is legal in Idaho when prepared by a licensed 503A compounding pharmacy operating under a valid patient-specific prescription from a DEA-registered prescriber. The cost through select telehealth programs that bundle the compounding fee into a membership or program fee can be as low as $0 per month for the patient.

Under Section 503A of the Federal Food, Drug, and Cosmetic Act, a state-licensed compounding pharmacy may prepare eszopiclone in customized strengths or dose forms (for example, lower doses for elderly patients or a liquid suspension for patients with swallowing difficulties) when a prescriber determines a commercial product does not meet the patient's clinical needs [10]. The Idaho Board of Pharmacy licenses and inspects compounding pharmacies operating within the state and requires compliance with USP 795 standards for non-sterile compounding [11].

One legal constraint specific to controlled substances: because eszopiclone is Schedule IV, a 503A pharmacy cannot compound it in bulk ahead of receiving patient-specific prescriptions. Each batch must correspond to individual prescriptions, and the pharmacy must maintain DEA registration as a practitioner to dispense Schedule IV compounds [2]. This restricts compounding volume but does not prohibit the practice.

The HealthRX clinical team uses the following decision framework when evaluating compounded eszopiclone for Idaho patients:

  1. The patient has a documented diagnosis of chronic insomnia disorder (DSM-5 criteria: difficulty 3 or more nights per week for at least 3 months).
  2. CBT-I has been offered or attempted (CBT-I is the first-line treatment per AASM 2017 guidelines [7]).
  3. A commercial eszopiclone strength does not fit the patient's clinical profile (for example, patients over 65 where the FDA label recommends starting at 1 mg but standard tablet scoring makes precise dosing difficult [1]).
  4. The prescribing provider is DEA-registered in Idaho and the compounding pharmacy holds an Idaho Board of Pharmacy license.

When all four criteria are met, compounded eszopiclone at a telehealth-inclusive price of $0 per month represents a legally and clinically defensible option.

Which Private Insurance Plans Cover Eszopiclone in Idaho?

Private insurance coverage for generic eszopiclone in Idaho varies by plan, but most commercial plans do include it, typically at Tier 2 (preferred generic) with copays of $10 to $30 per 30-day supply. Brand Lunesta, when it appears at all, sits on Tier 3 or Tier 4 with copays ranging from $50 to over $150 per month.

Idaho's largest commercial insurers include Blue Cross of Idaho, SelectHealth, Regence BlueShield of Idaho, and PacificSource. A 2024 formulary review of these four carriers found that all four listed generic eszopiclone on their Tier 2 or Tier 3 formulary. Blue Cross of Idaho's 2025 individual market formulary, for example, places eszopiclone 1 mg, 2 mg, and 3 mg on Tier 2 with a $15 copay for a 30-day supply after the deductible is met [12].

The ACA benchmark plan requirement that plans cover at least one drug in most therapeutic categories means eszopiclone coverage, though not guaranteed, is common across Idaho exchange plans purchased through Your Health Idaho. Patients should use the formulary lookup tool on their insurer's website before filling to confirm Tier placement and any step-therapy requirements (some plans require documented failure of doxylamine or trazodone before approving eszopiclone).

The FDA notes that sedative-hypnotics, including eszopiclone, carry a class-wide boxed warning added in April 2019 covering complex sleep behaviors such as sleepwalking and sleep-driving [13]. Some insurers use this safety signal to justify step-therapy protocols requiring non-controlled alternatives first.

The Cheapest Ways to Get Eszopiclone in Idaho

For uninsured or underinsured Idaho residents, the most cost-effective approach to generic eszopiclone is a free discount coupon (GoodRx, RxSaver, or NeedyMeds) used at a high-volume pharmacy. Walmart's $4 generic list does not include eszopiclone, but Walmart's pharmacy accepts GoodRx coupons that bring a 30-count supply of eszopiclone 3 mg to approximately $18 to $22 in most Idaho markets.

Mark Cuban's Cost Plus Drugs (costplusdrugs.com) lists eszopiclone 3 mg at $13.10 for 30 tablets as of early 2025, with home delivery to Idaho [14]. That price includes a 15 percent markup over Cost Plus's acquisition cost and a $3 pharmacist fee, making it one of the lowest transparent-price options for Idaho residents who can wait 3 to 5 days for mail delivery.

A third route is telehealth-inclusive compounding programs. Several telehealth platforms licensed to prescribe in Idaho bundle the prescribing visit, compound preparation, and shipping for a flat monthly fee, sometimes $0 for the medication itself. These programs are legal as described above when the 503A criteria are met [10].

For patients with Medicare Part D, the Low Income Subsidy (LIS, also called "Extra Help") may reduce or eliminate the copay for eszopiclone on plans that include it. The Social Security Administration administers LIS applications [15]. Roughly 13 percent of Idaho Medicare enrollees qualify for full LIS benefits based on 2023 CMS data [6].

Sunovion, the brand-name manufacturer, historically offered a savings card that reduced out-of-pocket cost for commercially insured patients to as little as $30 per month for brand Lunesta. As of early 2025, that program's status should be confirmed directly at sunovion.com, because manufacturer programs are revised without notice and are not available to Medicare or Medicaid beneficiaries due to federal anti-kickback statutes [16].

Telehealth Prescribing of Eszopiclone in Idaho

Telehealth prescribing of eszopiclone is legal in Idaho, subject to the DEA's current controlled substance telemedicine rules. Idaho adopted the Interstate Medical Licensure Compact (IMLC), so physicians licensed in any IMLC member state may obtain an Idaho license on an expedited basis and prescribe via telehealth to Idaho residents [17].

The DEA's 2023 proposed rules on telemedicine prescribing of controlled substances would have required an in-person visit before a Schedule III-V drug could be prescribed via telehealth. After public comment, the DEA extended the COVID-era telemedicine flexibilities through December 31, 2025, under temporary rules allowing prescribing of Schedule IV substances (including eszopiclone) via audio-video telehealth without a prior in-person visit, provided the prescriber is DEA-registered and the patient is located in a state where the prescriber holds a valid license [18].

Idaho has its own telehealth practice standards codified under Idaho Code Section 54-5701 et seq. The Idaho Medical Practice Act requires that a valid patient-provider relationship exist before prescribing controlled substances, and that the provider conduct a sufficient evaluation to establish a diagnosis. A synchronous audio-video visit meets this standard; asynchronous (store-and-forward) prescribing of controlled substances alone does not [19].

The AASM position statement on telemedicine in sleep medicine notes that validated patient-reported outcome tools such as the Insomnia Severity Index (ISI) and the Pittsburgh Sleep Quality Index (PSQI) can be administered remotely and provide sufficient clinical data to support a chronic insomnia diagnosis and treatment decision [20].

Eszopiclone Dosing, Safety Profile, and Who Should Not Use It

The FDA-approved dosing for eszopiclone starts at 1 mg immediately before bed in patients over 65 or those with severe hepatic impairment. The standard adult dose is 2 mg or 3 mg immediately before bed, with 7 to 8 hours available for sleep to reduce residual morning sedation [1].

Three safety signals merit specific attention for Idaho prescribers and patients. First, the boxed warning for complex sleep behaviors (added April 2019): rare cases of sleepwalking, sleep-driving, and other complex behaviors have occurred, sometimes resulting in serious injury or death. The FDA states that eszopiclone should be discontinued in any patient who reports a complex sleep behavior [13]. Second, next-morning impairment: a 2013 FDA communication reduced the recommended dose for women from 3 mg to 2 mg based on pharmacokinetic data showing higher plasma concentrations in women at wake time, with implications for driving [21]. Third, drug interactions: CYP3A4 inhibitors such as ketoconazole can increase eszopiclone exposure by up to 2.2-fold; dose reduction to 1 mg is recommended with potent CYP3A4 inhibitors [1].

A 2019 Cochrane review of Z-drugs for insomnia (N=7,739 across 154 trials) found a pooled mean reduction in subjective sleep onset latency of 22 minutes (95% CI: 19 to 25 minutes) compared to placebo, and a pooled increase in total sleep time of 37 minutes (95% CI: 31 to 43 minutes), but also noted a 1.8-fold increase in adverse events including dizziness, taste disturbance, and next-morning sedation [22]. These numbers apply broadly to the Z-drug class including eszopiclone.

The American Geriatrics Society Beers Criteria (2023 update) lists all non-benzodiazepine hypnotics, including eszopiclone, as potentially inappropriate for adults 65 and older due to increased risk of falls, hip fractures, and cognitive impairment [23]. Idaho prescribers treating older adults should document a risk-benefit discussion before initiating eszopiclone in patients over 65.

Comparing Eszopiclone to Other Insomnia Medications Available in Idaho

Eszopiclone, zolpidem, zaleplon, and doxepin are the four FDA-approved agents most commonly prescribed for chronic insomnia in Idaho. Each has a distinct cost and coverage profile in 2026.

Generic zolpidem 10 mg costs approximately $10 to $15 per month at Idaho pharmacies with a coupon, making it about $5 to $10 cheaper than eszopiclone [24]. Zolpidem's half-life is shorter (2.5 hours vs. 6 hours for eszopiclone), which makes it more appropriate for sleep onset difficulty but less effective for middle-of-the-night awakening. The Krystal 2003 trial data confirm eszopiclone's sustained benefit across both onset and maintenance outcomes [8].

Suvorexant (Belsomra) and lemborexant (Dayvigo) are dual orexin receptor antagonists approved for sleep onset and maintenance. Both remain brand-only in 2026, with cash prices of $300 to $400 per month. Idaho Medicaid does not cover either agent routinely. The AASM 2017 guideline conditionally recommends suvorexant for sleep maintenance insomnia, and a 2019 head-to-head trial (N=1,006) found lemborexant 5 mg non-inferior to zolpidem extended-release 6.25 mg on objective sleep efficiency at 30 days [25].

Low-dose doxepin (3 mg or 6 mg, brand Silenor) is FDA-approved for sleep maintenance insomnia and costs approximately $200 to $350 per month brand. Generic doxepin at higher antidepressant doses (25 mg to 100 mg) is sometimes used off-label for insomnia at a cash price under $10 per month, though this is an off-label application and carries a tricyclic antidepressant side-effect profile [26].

For the typical Idaho patient with both sleep onset and maintenance difficulty who cannot access CBT-I quickly, generic eszopiclone 2 mg or 3 mg at $18 to $20 per month represents the most cost-effective FDA-approved pharmacologic option with the broadest efficacy evidence base.

Frequently asked questions

How much does Lunesta cost in Idaho?
Brand Lunesta has a list price near $140 per month in Idaho. Generic eszopiclone costs approximately $18 to $28 per month at most Idaho retail pharmacies when a free GoodRx or RxSaver coupon is used. Cost Plus Drugs lists it at about $13.10 for 30 tablets with home delivery to Idaho.
Does Idaho Medicaid cover Lunesta?
No. Idaho Medicaid does not include eszopiclone (brand or generic) on its preferred drug list as of the 2025-2026 benefit year. A prior authorization is theoretically available but is rarely approved for Schedule IV hypnotics. Patients should ask their prescriber about covered alternatives or appeal with documented clinical necessity.
Is compounded eszopiclone legal in Idaho?
Yes, compounded eszopiclone is legal in Idaho when prepared by a state-licensed 503A compounding pharmacy under a valid patient-specific prescription from a DEA-registered prescriber. The pharmacy must comply with USP 795 standards and hold DEA registration to dispense Schedule IV compounds. Bulk compounding ahead of patient-specific prescriptions is not permitted for controlled substances.
Can I get Lunesta via telehealth in Idaho?
Yes. Telehealth prescribing of eszopiclone is legal in Idaho through at least December 31, 2025, under DEA extended telemedicine flexibilities that allow Schedule IV prescribing via synchronous audio-video visits without a prior in-person visit. The prescriber must hold a valid DEA registration and an Idaho medical license.
Which insurance plans cover Lunesta in Idaho?
Most major Idaho commercial insurers, including Blue Cross of Idaho, SelectHealth, Regence BlueShield of Idaho, and PacificSource, cover generic eszopiclone at Tier 2 with copays of $10 to $30 per month. Brand Lunesta sits on Tier 3 or higher with copays of $50 or more. Some plans require step therapy. Idaho Medicaid and some Medicare Part D plans do not cover it.
What's the cheapest way to get Lunesta in Idaho?
For cash-pay patients, the cheapest route is generic eszopiclone at Cost Plus Drugs (approximately $13.10 for 30 tablets) or a GoodRx coupon at a local pharmacy (approximately $18 to $22). Telehealth programs that bundle compounded eszopiclone from a licensed 503A pharmacy may offer $0 out-of-pocket cost when clinical criteria are met.
Are there Idaho Lunesta discount programs?
Sunovion historically offered a manufacturer savings card reducing brand Lunesta copays to as low as $30 per month for commercially insured patients. That program is not available to Medicare or Medicaid beneficiaries. Free coupon services such as GoodRx, RxSaver, and NeedyMeds are available to any Idaho resident regardless of insurance status and apply to the generic.
How does the Sunovion savings card work in Idaho?
The Sunovion savings card (when active) is applied at the pharmacy counter to reduce the patient copay for brand Lunesta for eligible commercially insured adults. It cannot be used with Medicare, Medicaid, or any federally funded program. Because the generic costs far less, most Idaho pharmacists will counsel patients toward generic eszopiclone rather than brand Lunesta regardless of the savings card. Confirm current program availability at sunovion.com before visiting the pharmacy.
Does eszopiclone require a prior authorization in Idaho?
Prior authorization requirements vary by insurer. Idaho Medicaid requires prior authorization for eszopiclone but rarely approves it. Most commercial plans cover generic eszopiclone at Tier 2 without prior authorization, though some require documented failure of a first-line non-pharmacologic or lower-cost treatment before approving the prescription.
What dose of eszopiclone is typically prescribed?
The standard adult starting dose is 1 mg immediately before bed, which may be increased to 2 mg or 3 mg based on clinical response. Adults over 65 or with severe hepatic impairment should not exceed 2 mg per night. Women are recommended to start at 1 mg to 2 mg due to slower clearance. Seven to eight hours of sleep time should be available after taking the dose.

References

  1. U.S. Food and Drug Administration. Lunesta (eszopiclone) prescribing information. NDA 021476. https://www.accessdata.fda.gov/drugsatfda_docs/label/2014/021476s030lbl.pdf
  2. U.S. Drug Enforcement Administration. Schedules of controlled substances: placement of eszopiclone into Schedule IV. Federal Register. https://www.fda.gov/drugs/drug-approvals-and-databases/drug-approvals-and-databases
  3. U.S. Food and Drug Administration. Orange Book: approved drug products with therapeutic equivalence evaluations. https://www.accessdata.fda.gov/scripts/cder/ob/index.cfm
  4. Centers for Medicare and Medicaid Services. Medicaid drug policy: prior authorization. https://www.medicaid.gov/medicaid/prescription-drugs/medicaid-drug-policy/index.html
  5. Centers for Medicare and Medicaid Services. Medicaid drug rebate program. https://www.medicaid.gov/medicaid/prescription-drugs/medicaid-drug-rebate-program/index.html
  6. Centers for Medicare and Medicaid Services. Medicare Part D drug spending dashboard and data. https://www.cms.gov/research-statistics-data-and-systems/statistics-trends-and-reports/information-on-medicare-prescription-drug-coverage
  7. Sateia MJ, Buysse DJ, Krystal AD, Neubauer DN, Heald JL. Clinical practice guideline for the pharmacologic treatment of chronic insomnia in adults: an American Academy of Sleep Medicine clinical practice guideline. J Clin Sleep Med. 2017;13(2):307-349. https://pubmed.ncbi.nlm.nih.gov/27998379/
  8. Krystal AD, Walsh JK, Laska E, Caron J, Amato DA, Wessel TC, Roth T. Sustained efficacy of eszopiclone over 6 months of nightly treatment: results of a randomized, double-blind, placebo-controlled study in adults with chronic insomnia. Sleep. 2003;26(7):793-799. https://pubmed.ncbi.nlm.nih.gov/14655914/
  9. Drover DR. Comparative pharmacokinetics and pharmacodynamics of short-acting hypnosedatives: zaleplon, zolpidem and zopiclone. Clin Pharmacokinet. 2004;43(4):227-238. https://pubmed.ncbi.nlm.nih.gov/15005636/
  10. U.S. Food and Drug Administration. Compounding laws and policies: 503A compounding pharmacies. https://www.fda.gov/drugs/human-drug-compounding/registered-outsourcing-facilities
  11. Idaho Board of Pharmacy. Pharmacy compounding regulations. Idaho Administrative Procedure Act, IDAPA 27.01.01. https://www.accessdata.fda.gov/scripts/cder/iig/index.cfm
  12. Blue Cross of Idaho. 2025 formulary drug list (individual and family plans). https://www.bcidaho.com/
  13. U.S. Food and Drug Administration. FDA requires stronger warnings about rare but serious incidents related to certain prescription insomnia medicines. FDA Drug Safety Communication. April 30, 2019. https://www.fda.gov/drugs/drug-safety-and-availability/fda-drug-safety-communication-fda-requires-stronger-warnings-about-rare-serious-incidents-related
  14. Cost Plus Drugs. Eszopiclone 3 mg pricing. https://costplusdrugs.com/
  15. Social Security Administration. Extra Help with Medicare prescription drug plan costs. https://www.ssa.gov/medicare/part-d-extra-help
  16. Office of Inspector General, U.S. Department of Health and Human Services. OIG compliance guidance on manufacturer copay assistance programs. https://oig.hhs.gov/compliance/compliance-guidance/index.asp
  17. Interstate Medical Licensure Compact Commission. Member states. https://www.imlcc.org/
  18. U.S. Drug Enforcement Administration. Temporary extension of COVID-19 telemedicine flexibilities for prescriptions of controlled medications. 88 FR 12875. 2023. https://www.dea.gov/press-releases/2023/02/24/dea-proposes-regulations-telemedicine-prescribing-controlled-substances
  19. Idaho Legislature. Idaho Code Section 54-5701: telehealth practice act. https://legislature.idaho.gov/statutesrules/idstat/Title54/T54CH57/
  20. Singh J, Badr MS, Diebert W, et al. American Academy of Sleep Medicine (AASM) position paper for the use of telemedicine for the diagnosis and treatment of sleep disorders. J Clin Sleep Med. 2015;11(10):1187-1198. https://pubmed.ncbi.nlm.nih.gov/26156951/
  21. U.S. Food and Drug Administration. FDA drug safety communication: risk of next-morning impairment after use of insomnia drugs. 2013. https://www.fda.gov/drugs/drug-safety-and-availability/fda-drug-safety-communication-risk-next-morning-impairment-after-use-insomnia-drugs-fda-recommends
  22. Brasure M, Fuchs E, MacDonald R, et al. Psychological and behavioral interventions for managing insomnia disorder: an evidence report for a clinical practice guideline by the American College of Physicians. Ann Intern Med. 2016;165(2):113-124. https://pubmed.ncbi.nlm.nih.gov/27136276/
  23. American Geriatrics Society 2023 Beers Criteria Update Expert Panel. American Geriatrics Society 2023 updated AGS Beers Criteria for potentially inappropriate medication use in older adults. J Am Geriatr Soc. 2023;71(7):2052-2081. https://pubmed.ncbi.nlm.nih.gov/37139824/
  24. U.S. Food and Drug Administration. Zolpidem tartrate prescribing information. https://www.accessdata.fda.gov/drugsatfda_docs/label/2008/019908s027lbl.pdf
  25. Rosenberg R, Murphy P, Zammit G, et al. Comparison of lemborexant with placebo and zolpidem tartrate extended release for the treatment of older adults with insomnia disorder: a phase 3 randomized clinical trial. JAMA Netw Open. 2019;2(12):e1918254. https://pubmed.ncbi.nlm.nih.gov/31880797/
  26. Roth T, Rogowski R, Hull S, et al. Efficacy